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Clinical trial protocol
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1	Microsoft Word - SOP editedonlineversibaru.doc Add to Reading List Source URL: www.ummc.edu.my Language: English - Date: 2015-06-03 21:28:52 Medical research Clinical research Pharmaceutical industry Institutional review board Clinical trial Good clinical practice Informed consent Adverse event Protocol Ethics committee Serious adverse event University Malaya Medical Centre
2	Determinants of young Adult Social well-being and Health A survey of young people from different ethnic groups in London http://www.facebook.com/dashlondon Protocol for tracing hard to reach DASH participants 1. Backgrou Add to Reading List Source URL: dash.sphsu.mrc.ac.uk Language: English - Date: 2016-08-23 09:05:20 Technology Medical research Digital media Pharmaceutical industry Email Text messaging Clinical trial Mobile phone Usability Dash
3	Instructions Questions? Contact the IRB Education Specialist atSee guidance GUI-6 and HRPP Policy Manual Chapter 5.9. Report to IRB The protocol director must submit the following to the IRB within five ( Add to Reading List Source URL: humansubjects.stanford.edu Language: English - Date: 2016-04-12 01:21:50 Medical research Medical ethics Research Health Autonomy Clinical research ethics Food and Drug Administration Informed consent Expanded access Investigational New Drug Consent Clinical trial
4	STANFORD UNIVERSITY – HIPAA Authorization Form Protocol Title: _______________________________________________________________ Protocol Director: __________________________________________________________________ Add to Reading List Source URL: humansubjects.stanford.edu Language: English - Date: 2016-04-12 01:21:57 Medical research Health Medicine Clinical research Medical ethics Health informatics Pharmaceutical industry Health Insurance Portability and Accountability Act Clinical trial Medical record Informed consent Human subject research
5	PROTOCOL NARRATIVE FOR EXEMPT RESEARCH University of California, Irvine Add to Reading List Source URL: www.research.uci.edu Language: English - Date: 2015-11-10 15:20:46 Medical research Health Clinical research Design of experiments Medical ethics Pharmaceutical industry Research ethics Institutional review board Clinical trial Human subject research Health Insurance Portability and Accountability Act Health informatics
6	DOD and HSRRB Specific Requirements Add to Reading List Source URL: mrmc.amedd.army.mil Language: English - Date: 2013-04-16 15:32:17 Medical research Clinical research Research Statistics Design of experiments Medical ethics Pharmaceutical industry Institutional review board Clinical trial Public Responsibility in Medicine and Research Human subject research Protocol
7	Stanford University Scientific Review Protocol for Human Subjects ResearchNOTResearch Compliance Office (for projects not otherwise undergoing Scientific Review) Template language for use by IRB Ma Add to Reading List Source URL: humansubjects.stanford.edu Language: English - Date: 2016-04-12 01:21:50 Design of experiments Scientific method Experiments Formal sciences Data Statistics Research Hypothesis Data analysis Statistical hypothesis testing Clinical trial
8	CHARGE TO THE ADMINISTRATIVE PANEL ON Add to Reading List Source URL: humansubjects.stanford.edu Language: English - Date: 2016-04-12 01:21:54 Clinical research Design of experiments Research ethics Medical ethics Public Responsibility in Medicine and Research Human subject research Clinical trial Common Rule Protocol
9	Stanford University Gene Transfer Protocol Application Supplemental Questions APP-12m 2/15 Locations of the Clinical Trial Add to Reading List Source URL: humansubjects.stanford.edu Language: English - Date: 2016-04-12 01:21:51 Clinical research Design of experiments Nursing research Medical ethics National Institutes of Health Clinical trial Institutional review board Appendix Human subject research Molecular cloning
10	CHG-3 CHARGE TO THE ADMINISTRATIVE PANELS ON HUMAN SUBJECTS IN MEDICAL RESEARCH BY THE VICE PROVOST AND DEAN OF RESEARCH (IRB/SCRO) (August 2015) Add to Reading List Source URL: researchcompliance.stanford.edu Language: English - Date: 2016-04-12 01:21:54 Clinical research Design of experiments Research ethics Medical ethics Public Responsibility in Medicine and Research Human subject research Clinical trial Common Rule Protocol